| scholarly article | Q13442814 |
| P50 | author | Benjamin Darbro | Q60912281 |
| John Manak | Q68533442 | ||
| Pedro Gonzalez-Alegre | Q88491589 | ||
| Heather C. Mefford | Q92098631 | ||
| Lily Paemka | Q96091586 | ||
| Naoto Ueno | Q54631561 | ||
| Thomas H Wassink | Q58048398 | ||
| John A Wemmie | Q58839805 | ||
| Keizō Takao | Q59453900 | ||
| Tsuyoshi Miyakawa | Q37381999 | ||
| Hatem El-shanti | Q42680338 | ||
| P2093 | author name string | Alexander G Bassuk | |
| Andrew A Pieper | |||
| Asuka Miyagi | |||
| Danielle S Rudd | |||
| Gemma L Carvill | |||
| Hirotaka Tao | |||
| Jeremiah K Britt | |||
| Jessica M Skeie | |||
| Levi P Sowers | |||
| Polly J Ferguson | |||
| Salleh N Ehaideb | |||
| Shu Wu | |||
| Toshikuni Sasaoka | |||
| Vinit B Mahajan | |||
| P2860 | cites work | Advances in autism genetics: on the threshold of a new neurobiology | Q22251023 |
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| Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene | Q24305575 | ||
| A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome | Q24310789 | ||
| The balance between isoforms of the prickle LIM domain protein is critical for planar polarity in Drosophila imaginal discs | Q24599652 | ||
| A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism | Q24643479 | ||
| Conditional calcineurin knockout mice exhibit multiple abnormal behaviors related to schizophrenia | Q24678573 | ||
| Toward a functional analysis of the yeast genome through exhaustive two-hybrid screens | Q28131836 | ||
| Autism spectrum disorders | Q28141851 | ||
| Identification and characterization of human PRICKLE1 and PRICKLE2 genes as well as mouse Prickle1 and Prickle2 genes homologous to Drosophila tissue polarity gene prickle | Q28202925 | ||
| Regulation of dense core vesicle release from PC12 cells by interaction between the D2 dopamine receptor and calcium-dependent activator protein for secretion (CAPS) | Q28247263 | ||
| LIM domains: multiple roles as adapters and functional modifiers in protein interactions | Q28271283 | ||
| Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders | Q28273097 | ||
| PSD-95 is associated with the postsynaptic density and not with the presynaptic membrane at forebrain synapses | Q28288026 | ||
| [The behavioral disorders in epilepsy] | Q78070184 | ||
| Prediction, assessment and validation of protein interaction maps in bacteria | Q78482210 | ||
| Expression of the neurosecretory process in PC12 cells is governed by REST | Q80768784 | ||
| Neuroethologically delineated differences in the seizure behavior of synapsin 1 and synapsin 2 knock-out mice | Q83211139 | ||
| PRICKLE1 progressive myoclonus epilepsy in Southern Italy | Q85032685 | ||
| SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function | Q45777752 | ||
| Valproic acid regulates catecholaminergic pathways by concentration-dependent threshold effects on TH mRNA synthesis and degradation | Q46270620 | ||
| Abnormality of circadian rhythm accompanied by an increase in frontal cortex serotonin in animal model of autism | Q48342915 | ||
| RNG105 deficiency impairs the dendritic localization of mRNAs for Na+/K+ ATPase subunit isoforms and leads to the degeneration of neuronal networks. | Q53299459 | ||
| Neurites from PC12 cells are connected to each other by synapse-like structures. | Q53461977 | ||
| The protein-protein interaction map of Helicobacter pylori | Q28484787 | ||
| Common increase of GATA-3 level in PC-12 cells by three teratogens causing autism spectrum disorders | Q28577640 | ||
| Association of mouse Dlg4 (PSD-95) gene deletion and human DLG4 gene variation with phenotypes relevant to autism spectrum disorders and Williams' syndrome | Q28586842 | ||
| Characteristics of a human cell line transformed by DNA from human adenovirus type 5 | Q29547863 | ||
| Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2 | Q29616085 | ||
| Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice | Q29618044 | ||
| Mouse model of Timothy syndrome recapitulates triad of autistic traits. | Q30474075 | ||
| Comprehensive behavioral phenotyping of calpastatin-knockout mice | Q30483897 | ||
| Mechanisms of prickle1a function in zebrafish epilepsy and retinal neurogenesis | Q30539146 | ||
| Protein interaction mapping: a Drosophila case study | Q33211911 | ||
| A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism | Q34064491 | ||
| The coxsackie B virus and adenovirus receptor resides in a distinct membrane microdomain | Q34471404 | ||
| Mutations in prickle orthologs cause seizures in flies, mice, and humans | Q34560912 | ||
| Mouse behavioral assays relevant to the symptoms of autism | Q34699041 | ||
| Yeast two-hybrid, a powerful tool for systems biology | Q34990983 | ||
| Exploring New Gene Discoveries in Idiopathic Generalized Epilepsy | Q35129602 | ||
| Genetic influences in childhood-onset psychiatric disorders: autism and attention-deficit/hyperactivity disorder | Q35250432 | ||
| Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsy | Q35444901 | ||
| The possible interplay of synaptic and clock genes in autism spectrum disorders | Q37141139 | ||
| Mouse prickle1, the homolog of a PCP gene, is essential for epiblast apical-basal polarity | Q37321035 | ||
| Circadian rhythms and sleep in children with autism | Q37644989 | ||
| The synapsins: key actors of synapse function and plasticity. | Q37741320 | ||
| Dystrophic serotonin axons in postmortem brains from young autism patients | Q37929093 | ||
| Zebrafish prickle, a modulator of noncanonical Wnt/Fz signaling, regulates gastrulation movements. | Q38520593 | ||
| Role of Prickle1 and Prickle2 in neurite outgrowth in murine neuroblastoma cells | Q39417564 | ||
| Mutations in the calcium-related gene IL1RAPL1 are associated with autism | Q39938403 | ||
| Mouse Prickle1 and Prickle2 are expressed in postmitotic neurons and promote neurite outgrowth | Q40080457 | ||
| Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives | Q40960910 | ||
| Modeling autism: a systems biology approach | Q42062971 | ||
| Targeting ASIC1a reduces innate fear and alters neuronal activity in the fear circuit. | Q42627546 | ||
| A system for characterizing cellular and molecular events in programmed neuronal cell death. | Q42809910 | ||
| The role of the dorsal hippocampus in the acquisition and retrieval of context memory representations. | Q44795491 | ||
| Aberrant cellular behavior of mutant torsinA implicates nuclear envelope dysfunction in DYT1 dystonia. | Q44804036 | ||
| P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | autism | Q38404 |
| autism spectrum disorder | Q1436063 | ||
| P304 | page(s) | e80737 | |
| P577 | publication date | 2013-01-01 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders | |
| P478 | volume | 8 |
| Q28079929 | A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons. |
| Q88782682 | A de novo mutation in PRICKLE1 associated with myoclonic epilepsy and autism spectrum disorder |
| Q36744640 | A de novo mutation in PRICKLE1 in fetal agenesis of the corpus callosum and polymicrogyria |
| Q38697548 | A proteomic analysis of LRRK2 binding partners reveals interactions with multiple signaling components of the WNT/PCP pathway |
| Q38491714 | Are Molecules Involved in Neuritogenesis and Axon Guidance Related to Autism Pathogenesis? |
| Q30583673 | Distinct motor impairments of dopamine D1 and D2 receptor knockout mice revealed by three types of motor behavior |
| Q54901806 | Dynamin 1 isoform roles in a mouse model of severe childhood epileptic encephalopathy. |
| Q31060238 | Epilepsy and Autism |
| Q47580007 | Epilepsy as a Network Disorder (1): What can we learn from other network disorders such as autistic spectrum disorder and mood disorders? |
| Q37612535 | Evidence for opposing roles of Celsr3 and Vangl2 in glutamatergic synapse formation |
| Q37496956 | Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders |
| Q89236147 | Extracellular superoxide dismutase (SOD3) regulates oxidative stress at the vitreoretinal interface |
| Q50047285 | Hub connectivity, neuronal diversity, and gene expression in the Caenorhabditis elegans connectome |
| Q64889423 | Linking Cell Polarity to Cortical Development and Malformations. |
| Q30374282 | Mutation of orthologous prickle genes causes a similar epilepsy syndrome in flies and humans. |
| Q38917986 | Neurodevelopmental Perspectives on Wnt Signaling in Psychiatry |
| Q37199039 | Olfactory stem cells reveal MOCOS as a new player in autism spectrum disorders |
| Q41512358 | Prickle1 regulates neurite outgrowth of apical spiral ganglion neurons but not hair cell polarity in the murine cochlea |
| Q28543984 | Seizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinase |
| Q38622672 | Single-Gene Determinants of Epilepsy Comorbidity |
| Q35705783 | Transcriptome Profiling of Peripheral Blood in 22q11.2 Deletion Syndrome Reveals Functional Pathways Related to Psychosis and Autism Spectrum Disorder |
| Q34002617 | prickle modulates microtubule polarity and axonal transport to ameliorate seizures in flies |
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